Angiopoietin-based interventions for treating cerebral malaria

ABSTRACT

The present invention provides methods for treating, preventing or reducing the severity of cerebral malaria. The methods of the present invention comprise administering to a subject in need thereof a therapeutically effective amount of a pharmaceutical composition comprising a modified angiopoietin molecule such as AngF1-Fc-F1.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a division of U.S. application Ser. No. 15/949,472, filed Apr. 10, 2018, now U.S. Pat. No. 10,251,938, which is a division of U.S. application Ser. No. 15/414,925, filed Jan. 25, 2017, now U.S. Pat. No. 9,968,653, which is a division of U.S. application Ser. No. 14/529,677, filed Oct. 31, 2014, now U.S. Pat. No. 9,592,271, which claims the benefit under 35 USC § 119(e) of US Provisional Application Nos. 61/898,539, filed on Nov. 1, 2013, and 62/040,514, filed on Aug. 22, 2014, the disclosures of which are each herein incorporated by reference in their entireties.

SEQUENCE LISTING

This application includes an electronic sequence listing in a file named “A0007US04-Sequence.txt”, created on Feb. 21, 2019 and containing 16,640 bytes, which is hereby incorporated by reference in its entirety for all purposes.

FIELD OF THE INVENTION

The present invention relates to the use of angiopoietin molecules or variants thereof to treat or prevent cerebral malaria in a subject in need thereof.

BACKGROUND

Cerebral malaria is a major cause of global morbidity and mortality, typically characterized by loss of blood brain barrier integrity and neurological impairment, followed by death in 15-30% cases despite treatment. Cerebral malaria in humans is caused by Plasmodium falciparum. The typical symptoms of cerebral malaria include fever, headache and myalgia followed by drowsiness, confusion, impaired balance or coordination, motor impairment, coma and death. Treatment options are currently limited to quinine or artemisinin derivatives, which control parasitemia but are not as effective in reducing mortality. Accordingly, an unmet need exists in the art for effective therapeutic and preventive approaches without adverse side-effects that prevent or treat cerebral malaria.

BRIEF SUMMARY OF THE INVENTION

According to one aspect of the present invention, methods are provided for treating, preventing or ameliorating at least one symptom, indication or complication of cerebral malaria (including, e.g., experimental cerebral malaria, falciparum malaria, etc.) in a subject. The methods according to this aspect of the invention comprise administering a therapeutically effective amount of a pharmaceutical composition comprising an angiopoietin or modified angiopoietin protein or a fragment thereof to a subject in need thereof.

In certain embodiments, the at least one symptom, indication or complication is selected from the group consisting of fever, headache and myalgia followed by drowsiness, confusion, vascular leakage, loss of blood-brain barrier integrity, elevated blood level of an endothelial marker, sequestration of parasitized erythrocytes in the brain, impaired balance or coordination, motor impairment, splenomegaly, loss of reflexes and self-preservation, lack of hygiene-related behavior, acute lung injury, convulsion, coma and death. In certain embodiments, the endothelial marker is selected from the group consisting of angiopoietin-1 (Ang1), angiopoietin-2 (Ang2), angiopoietin receptor Tie2, von Willebrand Factor (vWF), intercellular adhesion molecule-1 (ICAM-1), IP-10, E-selectin and vascular cell adhesion molecule-1 (VCAM-1).

According to another aspect of the present invention, methods are provided for improving or increasing survival of a subject following Plasmodium infection. The methods comprise administering a therapeutically effective amount of a pharmaceutical composition comprising an angiopoietin or modified angiopoietin protein or a fragment thereof to the subject in need thereof. In a related aspect, the invention provides methods for preventing vascular leakage or protecting blood brain barrier integrity, the method comprising administering a pharmaceutical composition comprising a therapeutically effective amount of an modified angiopoietin protein or a fragment thereof to a subject in need thereof.

In another aspect, the invention provides for methods for preventing severe cerebral malaria in a subject infected with Plasmodium spp., the method comprising selecting a subject with more than 0.1% parasitemia; and administering a pharmaceutical composition comprising a therapeutically effective amount of an modified angiopoietin protein or a fragment thereof to the subject in need thereof.

In certain embodiments, the administration of the modified angiopoietin to a subject in need thereof prevents at least one indication of neurological impairment selected from the group consisting of impaired balance or coordination, motor impairment, loss of reflexes and self-preservation, long term neurocognitive injury and impairment including memory deficits and affective disorders, lack of hygiene-related behavior, convulsion, and fitting or seizures.

In certain embodiments, the modified angiopoietin is administered in combination with a second therapeutic agent or therapy. In certain embodiments, the modified angiopoietin is administered as adjunctive therapy along with a second therapeutic agent such as e.g., artesunate.

Exemplary angiopoietin molecules that can be used in the context of the methods of the present invention include, e.g., angiopoietin-1, recombinant angiopoietin (e.g., angiopoietin-1 expressed in adenoviral vector), and a modified angiopoietin (e.g., a fusion protein comprising an angiopoietin or a fragment thereof). According to certain embodiments, the modified angiopoietin is a fusion protein consisting of the fibrinogen-like domain of angiopoietin fused to the Fc fragment of human IgG1 and then forced into a tetramer (Davis et al 2003, Nat. Struct. Biol. 10: 38-44). In certain embodiments, the modified angiopoietin comprises a fusion protein comprising a first fibrinogen-like domain of angiopoietin fused at its C-terminal end to the N-terminal end of an Fc fragment and the Fc fragment fused at its C-terminal end to the N-terminal end of a second fibrinogen-like domain of angiopoietin.

One such type of modified angiopoietin that can be used in the context of the methods of the present invention is AngF1-Fc-F1 (SEQ ID NO: 2).

In certain embodiments, the present invention provides use of an angiopoietin or a modified angiopoietin protein or a fragment thereof of the invention in the manufacture of a medicament to treat or inhibit or prevent cerebral malaria in a subject, including humans.

In another aspect, the present invention includes methods for treating, preventing or ameliorating at least one symptom, indication or complication of cerebral malaria (including, e.g., experimental cerebral malaria, falciparum malaria, etc.) in a subject. The methods according to this aspect of the invention comprise administering a therapeutically effective amount of a pharmaceutical composition comprising an anti-Tie2 antibody or an antigen-binding fragment thereof to a subject in need thereof. In certain embodiments, the anti-Tie2 antibody is an activating or agonist antibody.

Other embodiments of the present invention will become apparent from a review of the ensuing detailed description.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 shows the survival curves of C57Bl/6 (Experimental Cerebral Malaria-Susceptible; ECM-S) and BALB/c (Experimental Cerebral Malaria-Resistant; ECM-R) mice infected with Plasmodium berghei ANKA (PbA).

FIG. 2 shows the percent fold change in Rapid Murine Coma and Behavioral Score (RMCBS) in ECM-S and ECM-R mice infected with PbA.

FIG. 3 shows comparative levels of Evans Blue dye extracted from the brains of ECM-R and ECM-S mice infected with PbA.

FIG. 4 shows percent parasitemia in ECM-S and ECM-R mice infected with PbA.

FIG. 5 shows Ang-1 serum levels over the course of PbA infection. ***p<0.0001 (time), *p<0.05 (strain) and **p<0.001 (2-way ANOVA with Bonferroni post-test for the indicated comparison).

FIGS. 6(a) and 6(b): FIG. 6(a) RMCBS (%) and serum Ang-1 levels (ng/ml)*p<0.05 compared to naïve, One-way ANOVA. FIG. 6(b) depicts scatter plots showing linear regression analysis between serum Ang1 (ng/ml) levels and time to death (hours) (Spearman correlation, r value, p<0.0001).

FIG. 7 shows relative Ang2 protein levels in ECM-R and ECM-S mice post PbA infection.

FIG. 8 shows vWF protein levels in ECM-R and ECM-S mice on Day 6 post infection with PbA.

FIG. 9 shows the relative Tie2 mRNA levels in ECM-R and ECM-S mice post PbA infection.

FIG. 10 shows the survival curves of C57Bl/6 mice infected with PbA and treated with anti-Ang2 antibody (mAb isotype control (mAb ‘A’) or saline.

FIG. 11 shows percent fold change in RMCBS in C57Bl/6 mice infected with PbA and treated with anti-Ang2 antibody (mAb isotype control (mAb ‘A’) or saline.

FIG. 12 shows percent parasitemia on Day 7 post PbA infection in C57Bl/6 mice treated with anti-Ang2 antibody (mAb isotype control (mAb ‘A’) or saline.

FIGS. 13(a) and 13(b) show the plasma protein levels of (FIG. 13(a)) vWF and (FIG. 13(b)) E-selectin, ICAM and VCAM in naïve C57Bl/6 mice (hatched bars) or mice infected with PbA and treated with anti-Ang2 antibody (mAb ‘B’) (grey bars) or isotype control (mAb ‘A’) (black bars).

FIG. 14 shows survival curves of C57Bl/6 mice infected with PbA and treated with AngF1-Fc-F1, Fc control, anti-Ang2 antibody, a dual Anti-Ang1/Ang2 antibody (“comparator”) or saline.

FIG. 15 shows percent parasitemia in C57Bl/6 mice infected with PbA and treated with AngF1-Fc-F1, Fc control, anti-Ang2 antibody, a dual Anti-Ang1/Ang2 antibody (“comparator”) or saline.

FIGS. 16(a) and 16(b): FIG. 16(a) shows levels of Evans Blue dye extracted from the brains of C57Bl/6 mice infected with PbA and treated with Fc control (A), anti-Ang2 antibody (B), AngF1-Fc-F1 (C), or anti-Ang1/Ang2 comparator antibody (D). FIG. 16(b) shows the percent parasitemia in C57Bl/6 mice infected with PbA and treated with Fc control (A), anti-Ang2 antibody (B), AngF1-Fc-F1 (C), or anti-Ang1/Ang2 “comparator” antibody (D).

FIGS. 17(a) and 17(b): FIG. 17(a) shows the percent change in RMCBS on Day 6 post PbA infection in C57Bl/6 mice treated with AngF1-Fc-F1 or isotype control. FIG. 17(b) shows the percent change over 7 days in RMCBS in C57Bl/6 mice infected with PbA and treated with AngF1-Fc-F1 or isotype control.

FIGS. 18(a) and 18(b): FIG. 18(a) shows percent parasitemia in C57Bl/6 mice infected with PbA and treated with AngF1-Fc-F1 or isotype control. FIG. 18(b) shows the percent fold change in weight of C57Bl/6 mice infected with PbA and treated with AngF1-Fc-F1 or isotype control.

FIGS. 19(a), 19(b) and 19(c): FIG. 19 shows plasma protein levels of cytokines TNFα and IFNγ (a), vWF (b), E-selectin, sICAM and VCAM-1 (c) of naïve C57Bl/6 mice and mice infected with PbA and treated with AngF1-Fc-F1 or Fc control.

FIG. 20 shows survival curves of C57Bl/6 mice infected with PbA and treated with artesunate+AngF1-Fc-F1, artesunate+saline, or saline.

FIGS. 21(a) and 21(b): FIG. 21(a) shows percent parasitemia in C57Bl/6 mice infected with PbA and treated with artesunate+AngF1-Fc-F1 or artesunate+saline. FIG. 21(b) shows the percent fold change in weight of C57Bl/6 mice infected with PbA and treated with artesunate+AngF1-Fc-F1 or artesunate+saline.

DETAILED DESCRIPTION

Before the present invention is described, it is to be understood that this invention is not limited to particular methods and experimental conditions described, as such methods and conditions may vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting, since the scope of the present invention will be limited only by the appended claims.

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. As used herein, the term “about,” when used in reference to a particular recited numerical value, means that the value may vary from the recited value by no more than 1%. For example, as used herein, the expression “about 100” includes 99 and 101 and all values in between (e.g., 99.1, 99.2, 99.3, 99.4, etc.).

Although any methods and materials similar or equivalent to those described herein can be used in the practice of the present invention, the preferred methods and materials are now described. All publications mentioned herein are incorporated herein by reference to describe in their entirety.

Methods for Treating, Preventing or Ameliorating Cerebral Malaria

Cerebral malaria pathogenesis is associated with endothelial activation and loss of blood brain barrier integrity. The angiopoietin-Tie2 signaling pathway is a key regulator of endothelial function. Alterations in the angiogenic balance, specifically increased angiopoietin-2 (Ang2) relative to Ang1, has been associated with poor clinical outcome in cerebral malaria (Yeo et al, 2008 PNAS; Lovegrove et al PLoS ONE 2009; Erdman et al PLoS ONE 2011; Conroy et al PLoS ONE 2011). However, it is unclear whether the Ang-Tie2 pathway is causally involved in cerebral malaria pathogenesis. The inventors have hypothesized that dysregulation in angiopoietins contributes to cerebral malaria pathogenesis, and therefore, interventions to maintain Tie2 activation may promote endothelial stability, prevent deleterious effects to the blood brain barrier and improve outcome following Plasmodium infection. Accordingly, it is shown herein, that modified angiopoietins, when administered to an infected subject, protect the blood brain barrier integrity and prevent neurological impairment and death. As disclosed elsewhere herein, the inventors have used a well-known murine model of Plasmodium berghei ANKA (PbA)—induced experimental cerebral malaria (ECM) to study alterations in angiopoietins associated with disease severity and fatality and to show that dysregulation of the Ang/Tie2 axis is associated with disease severity and fatality. As shown herein, Ang1 levels inversely correlated with morbidity and mortality in the mouse model of cerebral malaria. Based on the studies shown herein, it is established that Ang1 is necessary to maintain blood brain barrier integrity in response to a lethal malaria challenge and can improve survival above that achieved by conventional treatment (e.g., artesunate) alone. Further, administration of a modified angiopoietin enhanced blood brain barrier integrity and promoted maintenance of a quiescent endothelium via down-regulation of pro-adhesive molecules implicated in parasite sequestration and cerebral malaria pathogenesis.

Accordingly, the present invention includes methods for treating, preventing, or ameliorating at least one symptom, indication or complication of cerebral malaria (including, for example, experimental cerebral malaria, falciparum malaria, etc.) in a subject. The methods according to this aspect of the invention comprise administering a therapeutically effective amount of a pharmaceutical composition comprising a modified angiopoietin protein or a fragment thereof to the subject in need thereof.

“Cerebral malaria” (CM), as used herein, means an infectious disease caused by Plasmodium species and characterized by loss of blood brain barrier integrity and neurological impairment. The symptoms of CM include, but are not limited to, fever, headache and myalgia followed by drowsiness, confusion, vascular leakage, loss of blood-brain barrier integrity, elevated blood level of an endothelial marker, sequestration of parasitized erythrocytes in the brain, impaired balance or coordination, motor impairment, splenomegaly, loss of reflexes and self-preservation, lack of hygiene-related behavior, acute lung injury, convulsion, fitting, coma and death. The clinicopathology of CM is characterized by sequestration of infected red blood cells in the venules and capillaries of the brain followed by endothelial activation. The term “cerebral malaria” includes but is not limited to severe cerebral malaria caused in humans by Plasmodium falciparum, and experimental cerebral malaria (ECM), caused in mice by Plasmodium berghei ANKA.

As used herein, the terms “treat”, “treating”, or the like, mean to alleviate a symptom or a complication, eliminate the causation of a symptom or a complication either on a temporary or permanent basis, or to prevent or slow the appearance of a symptom or complication of cerebral malaria in the subject. In the context of the present invention, the terms “treat”, “treating”, or the like, refer to reducing or decreasing mortality in a subject infected with Plasmodium species. The terms also refer to preventing the loss of blood brain barrier integrity and neurological impairment in a subject with cerebral malaria. In certain embodiments, the present methods are useful for treating or ameliorating at least one symptom, indication or complication of cerebral malaria including, but not limited to, fever, headache and myalgia followed by drowsiness, confusion, vascular leakage, loss of blood-brain barrier integrity, elevated blood level of an endothelial marker, sequestration of parasitized erythrocytes in the brain, impaired balance or coordination, motor impairment, splenomegaly, loss of reflexes and self-preservation, lack of hygiene-related behavior, acute lung injury, convulsion, fitting, coma and death.

By the phrase “therapeutically effective amount” is meant an amount that produces the desired effect for which it is administered. The exact amount will depend on the purpose of the treatment, and will be ascertainable by one skilled in the art using known techniques (see, for example, Lloyd (1999) The Art, Science and Technology of Pharmaceutical Compounding).

As used herein, the term “subject” refers to an animal, preferably a mammal, that exhibits one or more symptoms, indications or complications of cerebral malaria, and/or who has been diagnosed with cerebral malaria (CM) and/or in need of amelioration, prevention and/or treatment of cerebral malaria. The term “a subject in need thereof” may also include, e.g., subjects who, prior to treatment, exhibit (or have exhibited) one or more symptoms or indications of cerebral malaria such as, e.g., fever, headache and myalgia followed by drowsiness, confusion, vascular leakage, loss of blood-brain barrier integrity, elevated blood level of an endothelial marker, sequestration of parasitized erythrocytes in the brain, impaired balance or coordination, motor impairment, splenomegaly, loss of reflexes and self-preservation, lack of hygiene-related behavior, acute lung injury, convulsion, fitting, coma and death.

In the context of the present invention, “a subject in need thereof” may include a subset of population, which may show an elevated level of an endothelial marker. Such a subject population may show an elevated level of an endothelial marker such as, e.g., Ang1, Ang2, Tie2, vWF, ICAM-1, E-selectin and VCAM-1.

The methods of the present invention may be used to treat cerebral malaria in adults, including the elderly. In some embodiments, the methods of the present invention are used to treat adults more than 50 years, more than 55 years, more than 60 years, more than 65 years, or more than 70 years old.

In some embodiments, the methods herein may be used to treat cerebral malaria in children who are ≥3 years old. For example, the present methods may be used to treat infants who are less than 1 month, 2 months, 3 months, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months, 10 months, 11 months or less than 12 months old. In other embodiments, the methods of the present invention may be used to treat children who are more than 3 years old, more than 4 years, 5 years, 6 years, 7 years, 8 years, 9 years, 10 years, 11 years, 12 years, 13 years, 14 years, or more than 15 years old.

The present invention also includes methods for increasing survival in a subject with cerebral malaria. The methods according to this aspect of the invention comprise administering to the subject one or more doses of a pharmaceutical composition comprising a modified angiopoietin to increase survival in the subject.

The present invention also includes methods to prevent severe cerebral malaria in a subject infected with Plasmodium species, the methods comprising administering a therapeutically effective amount of a pharmaceutical composition comprising a modified angiopoietin to the subject in need thereof. In certain embodiments, the modified angiopoietin is administered as an exogenous protein.

The term “preventing” as used herein refers to preventing development of disease. The term, as used herein, also includes preventing vascular leakage, protecting blood brain barrier integrity and the onset of neurological symptoms such as seizures and paralysis upon infection with the pathogen. In some embodiments, the term refers to preventing endothelial dysfunction, which is a key pathological feature of cerebral malaria (including experimental cerebral malaria).

The present invention includes methods for treating, preventing or reducing the severity of cerebral malaria comprising administering a therapeutically effective amount of a pharmaceutical composition comprising a modified angiopoietin to a subject in need thereof, wherein the pharmaceutical composition is administered to the subject in multiple doses, e.g., as part of a specific therapeutic dosing regimen. For example, the therapeutic dosing regimen may comprise administering multiple doses of the pharmaceutical composition to the subject at a frequency of about once a day, once every two days, once every three days, once every four days, once every five days, once every six days, once a week, once every two weeks, once every three weeks, once every four weeks, once a month, once every two months, once every three months, once every four months, or less frequently. In some embodiments, the therapeutic dosing regimen comprises administering multiple doses of the pharmaceutical composition to the subject at a frequency of about once a day, about 2 times a day, about 3 times a day or more than 4 times a day.

In certain embodiments, the modified angiopoietin is administered subcutaneously, intravenously, intracranially, intraventricularly, or delivered systemically in an adenoviral vector to a subject in need thereof.

The methods of the present invention, according to certain embodiments, comprise administering to a subject a therapeutically effective amount of a pharmaceutical composition comprising a modified angiopoietin in combination with a second therapeutic agent. The second therapeutic agent may be an agent selected from the group consisting of an artemisinin, quinine, or a variant or derivative thereof (e.g., artesunate), a vascular endothelial growth factor (VEGF) antagonist [e.g., a “VEGF-Trap” such as aflibercept or other VEGF-inhibiting fusion protein as set forth in U.S. Pat. No. 7,087,411, or an anti-VEGF antibody or antigen binding fragment thereof (e.g., bevacizumab, or ranibizumab)], an activating anti-Tie2 antibody, an Ang2 antagonist, an antihistamine, and a non-steroidal anti-inflammatory drug (NSAID). As used herein, the phrase “in combination with” means that the pharmaceutical composition comprising a modified angiopoietin is administered to the subject at the same time as, just before, or just after administration of the second therapeutic agent. In certain embodiments, the second therapeutic agent is administered as a co-formulation with the modified angiopoietin.

The present invention also includes methods for treating, preventing or ameliorating at least one symptom, indication or complication of cerebral malaria in a subject, wherein the methods comprise administering a therapeutically effective amount of a pharmaceutical composition comprising an anti-Tie2 antibody or an antigen-binding fragment thereof to the subject in need thereof. In certain embodiments, the anti-Tie2 antibody is an activating or agonist antibody, e.g., the antibody upon binding to Tie2 increases the activity of Tie2 or otherwise stimulates Tie2 signaling. In certain embodiments, the anti-Tie2 antibody is an antibody as set forth in US20130209492. The anti-Tie2 antibody may be administered subcutaneously, intravenously, or intracranially at a dosage of from about 0.1 mg/kg to about 100 mg/kg of the subject's body weight. In certain embodiments, the activating anti-Tie2 antibody is administered in combination with a second activating anti-Tie2 antibody to the subject in need thereof.

In another aspect, the present invention includes methods for treating, preventing or ameliorating at least one symptom, indication or complication of a disease or disorder associated with dysfunction of the Ang-Tie2 pathway in a subject. The methods comprise administering a therapeutically effective amount of a pharmaceutical composition comprising a modified angiopoietin protein or a fragment thereof to the subject in need thereof. In certain embodiments, the angiopoietin or variants thereof may be used to treat, prevent or ameliorate at least one symptom or indication of a disease or disorder including cerebral malaria, sepsis, anthrax, dengue, hemorrhagic fever (including viral hemorrhagic fever, e.g., lassa fever, Yellow fever, and Ebola fever), toxic shock syndrome, HUS, hemorrhagic shock (model for massive blood loss due to traumatic injury, e.g., IED), ischemic reperfusion, hemolytic uremic syndrome, myocardial infarction and stroke.

Modified Angiopoietins

The methods of the present invention comprise administering to a subject in need thereof a therapeutic composition comprising an angiopoietin or a variant thereof. As used herein, an “angiopoietin” includes angiopoietin-1 (Ang1) or angiopoietin-2 (Ang2).

Non-limiting examples of categories of modified angiopoietins include recombinant angiopoietins (e.g., angiopoietin expressed in an adenoviral vector; Thurston et al 2000, Nat. Med.), mutant and chimeric forms of angiopoietins, and fusion proteins comprising angiopoietin or a fragment thereof that specifically bind Tie1 and/or Tie2 receptors.

According to certain exemplary embodiments of the present invention, the modified angiopoietin is a fusion protein comprising one or more domains of the angiopoietin molecule fused to a multimerizing domain. In general terms, the multimerizing domain(s) of the present invention function to connect the various components of the angiopoietin molecule (e.g., the fibrinogen-like domains) with one another. As used herein, a “multimerizing domain” is any macromolecule that has the ability to associate (covalently or non-covalently) with a second macromolecule of the same or similar structure or constitution. For example, a multimerizing domain may be a polypeptide comprising an immunoglobulin C_(H)3 domain. A non-limiting example of a multimerizing domain is an Fc portion of an immunoglobulin, e.g., an Fc domain of an IgG selected from the isotypes IgG1, IgG2, IgG3, and IgG4, as well as any allotype within each isotype group. In certain embodiments, the multimerizing domain is an Fc fragment or an amino acid sequence of 1 to about 200 amino acids in length containing at least one cysteine residues. In other embodiments, the multimerizing domain is a cysteine residue or a short cysteine-containing peptide. Other multimerizing domains include peptides or polypeptides comprising or consisting of a leucine zipper, a helix-loop motif, or a coiled-coil motif.

In certain embodiments, the modified angiopoietin is a fusion protein comprising one or more fibrinogen-like domains of the angiopoietin-1 molecule fused to the Fc fragment of an immunoglobulin comprising any of the amino acid sequences, as set forth in U.S. Pat. No. 7,008,781. In certain exemplary embodiments, the fusion protein that can be used in the context of the methods of the present invention comprises a first fibrinogen-like domain of angiopoietin fused at its C-terminal end to the N-terminal end of an IgG Fc fragment and the C-terminal of the Fc fragment fused to the N-terminal end of a second fibrinogen-like domain of angiopoietin (Davis et al, Nat. Struct. Biol. 2003), wherein the angiopoietin may be Ang1 or Ang2. According to certain exemplary embodiments, the methods of the present invention comprise the use of the modified angiopoietin referred to and known in the art as AngF1-Fc-F1. In certain embodiments, the modified angiopoietin is a dimer comprising two AngF1-Fc-F1s that associate through intramolecular association of the Fc fragments (also referred to as BowAng1, as disclosed in Davis et al, Nat. Struct. Biol. 2003). According to certain embodiments, the fusion protein comprises the amino acid sequence of SEQ ID NO: 2. In some embodiments, the fusion protein comprises the amino acid sequence of SEQ ID NO: 4.

Other modified angiopoietins that can be used in the context of the methods of the present invention include any of the modified angiopoietin molecules as set forth in U.S. Pat. Nos. 6,265,564, 6,441,137, and 6,825,008.

In certain embodiments, the angiopoietin or variants thereof may be used to treat, prevent or ameliorate at least one symptom or indication of a disease or disorder including sepsis, dengue, hemorrhagic fever (including viral hemorrhagic fever, e.g., lassa fever, Yellow fever, and Ebola fever), toxic shock syndrome, HUS, hemorrhagic shock (model for massive blood loss due to traumatic injury, e.g., IED), ischemic repurfusion, hemolytic uremic syndrome, myocardial infarction and stroke.

Pharmaceutical Compositions

The present invention includes methods which comprise administering a modified angiopoietin to a subject wherein the modified angiopoietin is contained within a pharmaceutical composition. The pharmaceutical compositions of the invention may be formulated with suitable carriers, excipients, and other agents that provide suitable transfer, delivery, tolerance, and the like. A multitude of appropriate formulations can be found in the formulary known to all pharmaceutical chemists: Remington's Pharmaceutical Sciences, Mack Publishing Company, Easton, Pa. These formulations include, for example, powders, pastes, ointments, jellies, waxes, oils, lipids, lipid (cationic or anionic) containing vesicles (such as LIPOFECTIN™), DNA conjugates, anhydrous absorption pastes, oil-in-water and water-in-oil emulsions, emulsions carbowax (polyethylene glycols of various molecular weights), semi-solid gels, and semi-solid mixtures containing carbowax. See also Powell et al. “Compendium of excipients for parenteral formulations” PDA (1998) J Pharm Sci Technol 52:238-311.

Various delivery systems are known and can be used to administer the pharmaceutical composition of the invention, e.g., encapsulation in liposomes, microparticles, microcapsules, recombinant cells capable of expressing the mutant viruses, receptor mediated endocytosis (see, e.g., Wu et al., 1987, J. Biol. Chem. 262: 4429-4432). Methods of administration include, but are not limited to, intradermal, intramuscular, intraperitoneal, intravenous, subcutaneous, intranasal, epidural, and oral routes. The composition may be administered by any convenient route, for example by infusion or bolus injection, by absorption through epithelial or mucocutaneous linings (e.g., oral mucosa, rectal and intestinal mucosa, etc.) and may be administered together with other biologically active agents.

A pharmaceutical composition of the present invention can be delivered subcutaneously or intravenously with a standard needle and syringe. In addition, with respect to subcutaneous delivery, a pen delivery device readily has applications in delivering a pharmaceutical composition of the present invention. Such a pen delivery device can be reusable or disposable. A reusable pen delivery device generally utilizes a replaceable cartridge that contains a pharmaceutical composition. Once all of the pharmaceutical composition within the cartridge has been administered and the cartridge is empty, the empty cartridge can readily be discarded and replaced with a new cartridge that contains the pharmaceutical composition. The pen delivery device can then be reused. In a disposable pen delivery device, there is no replaceable cartridge. Rather, the disposable pen delivery device comes prefilled with the pharmaceutical composition held in a reservoir within the device. Once the reservoir is emptied of the pharmaceutical composition, the entire device is discarded.

In certain situations, the pharmaceutical composition can be delivered in a controlled release system. In one embodiment, a pump may be used. In another embodiment, polymeric materials can be used; see, Medical Applications of Controlled Release, Langer and Wise (eds.), 1974, CRC Pres., Boca Raton, Fla. In yet another embodiment, a controlled release system can be placed in proximity of the composition's target, thus requiring only a fraction of the systemic dose (see, e.g., Goodson, 1984, in Medical Applications of Controlled Release, supra, vol. 2, pp. 115-138). Other controlled release systems are discussed in the review by Langer, 1990, Science 249:1527-1533.

The injectable preparations may include dosage forms for intravenous, subcutaneous, intracutaneous and intramuscular injections, drip infusions, etc. These injectable preparations may be prepared by known methods. For example, the injectable preparations may be prepared, e.g., by dissolving, suspending or emulsifying the antibody or its salt described above in a sterile aqueous medium or an oily medium conventionally used for injections. As the aqueous medium for injections, there are, for example, physiological saline, an isotonic solution containing glucose and other auxiliary agents, etc., which may be used in combination with an appropriate solubilizing agent such as an alcohol (e.g., ethanol), a polyalcohol (e.g., propylene glycol, polyethylene glycol), a nonionic surfactant [e.g., polysorbate 80, HCO-50 (polyoxyethylene (50 mol) adduct of hydrogenated castor oil)], etc. As the oily medium, there are employed, e.g., sesame oil, soybean oil, etc., which may be used in combination with a solubilizing agent such as benzyl benzoate, benzyl alcohol, etc. The injection thus prepared is preferably filled in an appropriate ampoule.

Advantageously, the pharmaceutical compositions for oral or parenteral use described above are prepared into dosage forms in a unit dose suited to fit a dose of the active ingredients. Such dosage forms in a unit dose include, for example, tablets, pills, capsules, injections (ampoules), suppositories, etc.

Dosage

The amount of the modified angiopoietin (e.g., AngF1-Fc-F1) administered to a subject according to the methods of the present invention is, generally, a therapeutically effective amount. As used herein, the phrase “therapeutically effective amount” means an amount of modified angiopoietin that results in one or more of: (a) a reduction in the severity or duration of a symptom, indication or complication of severe cerebral malaria; (b) increased survival; (c) protection of the blood brain barrier integrity; and (d) prevention of neurological impairment in the subject.

In the case of a modified angiopoietin, a therapeutically effective amount can be from about 0.05 mg to about 600 mg, e.g., about 0.05 mg, about 0.1 mg, about 1.0 mg, about 1.5 mg, about 2.0 mg, about 10 mg, about 20 mg, about 30 mg, about 40 mg, about 50 mg, about 60 mg, about 70 mg, about 80 mg, about 90 mg, about 100 mg, about 110 mg, about 120 mg, about 130 mg, about 140 mg, about 150 mg, about 160 mg, about 170 mg, about 180 mg, about 190 mg, about 200 mg, about 210 mg, about 220 mg, about 230 mg, about 240 mg, about 250 mg, about 260 mg, about 270 mg, about 280 mg, about 290 mg, about 300 mg, about 310 mg, about 320 mg, about 330 mg, about 340 mg, about 350 mg, about 360 mg, about 370 mg, about 380 mg, about 390 mg, about 400 mg, about 410 mg, about 420 mg, about 430 mg, about 440 mg, about 450 mg, about 460 mg, about 470 mg, about 480 mg, about 490 mg, about 500 mg, about 510 mg, about 520 mg, about 530 mg, about 540 mg, about 550 mg, about 560 mg, about 570 mg, about 580 mg, about 590 mg, or about 600 mg, of the modified angiopoietin.

The amount of the modified angiopoietin contained within the individual doses may be expressed in terms of milligrams of protein per kilogram of the subject's body weight (i.e., mg/kg). For example, the modified angiopoietin may be administered to a subject at a dose of about 0.0001 to about 100 mg/kg of patient body weight. In certain embodiments, the modified angiopoietin is administered to a subject in need thereof at a dose of about 5-25 mg/kg of the subject's body weight.

EXAMPLES

The following examples are put forth so as to provide those of ordinary skill in the art with a complete disclosure and description of how to make and use the methods and compositions of the invention, and are not intended to limit the scope of what the inventors regard as their invention. Efforts have been made to ensure accuracy with respect to numbers used (e.g., amounts, temperature, etc.) but some experimental errors and deviations should be accounted for. Unless indicated otherwise, parts are parts by weight, molecular weight is average molecular weight, temperature is in degrees Centigrade, and pressure is at or near atmospheric.

Example 1: Alterations in Endothelial Regulators in the Murine Plasmodium berghei ANKA (Pba)-Induced Model of Experimental Cerebral Malaria (ECM)

In this Example, the alterations in endothelial regulators in Plasmodium berghei ANKA (PbA)-induced experimental cerebral malaria in a mouse model were studied. This model is based on the observation that C57Bl/6 mice are susceptible to the murine parasite P. berghei ANKA which produces a severe, ultimately fatal disease with neurological symptoms paralleling the symptoms and disease development of cerebral malaria in humans infected with Plasmodium falciparum. In contrast to C57Bl/6 mice, BALB/c mice are resistant to PbA, in that they do not develop encephalopathy, although they become infected and achieve similar or sometimes higher levels of parasite density. This study showed that dysregulation of the Ang/Tie2 axis was associated with disease severity and fatality. Further, Ang1 levels inversely correlated with morbidity and mortality in the mouse model of cerebral malaria.

Materials and Methods

PbA-Induced ECM Model: Infection

Cryopreserved Plasmodium berghei ANKA (PbA; MR4, Manassas, Va.) was passaged through naïve C57Bl/6 mice. For the experiment, infection was initiated in C57Bl/6 and BALB/c mice by intraperitoneal (ip) injection of 1×10⁶ freshly-isolated parasitized erythrocytes (PE) obtained from donor passage mice. Parasitemia was monitored by thin-blood smear stained with modified Geimsa stain (Protocol Hema3 Stain Set, Sigma, Oakville, ON) by counting at least 1500 erythrocytes. The infected mice were monitored for survival, neurological impairment, vascular leakage, parasite burden, and levels of angiogenic factors and markers of endothelial activation.

Survival and Assessment of Health Status

Post-infection survival of mice was plotted as Kaplan Meier curves using a log rank test for comparison. Quantitative assessment of ECM-associated neurological impairment (impaired coordination and motor performance) was performed daily using the 10 parameter Rapid Murine Coma and Behavioral Score (RMCBS), as previously described by Carroll R W, et al. 2010 in PLoS ONE 5: e13124. Signs of ECM include impaired balance/coordination, motor impairment (ataxia, hemiplegia/paraplegia), loss of reflexes and self-preservation, lack of hygiene-related behavior (grooming) and/or fitting. For each parameter, a score was assigned from 0 to 2, with 0 indicating the lowest function and a score of 2 the highest. Total scores for each mouse were calculated and provided as a percentage of the total possible score. Mice with a score of 35% or less were deemed to have severe ECM.

Evans Blue Permeability Assay

Vascular permeability in the brain was assessed using Evans blue (EB) dye. Mice were intravenously injected via tail vein with 0.1 mL of 1% Evans blue dye solution (Evans Blue powder; Sigma-Aldrich in PBS, filter sterilized) when clinical signs of ECM were observed. Mice were euthanized with isoflurane (99.9% inhalational anesthetic) after 1 hour, perfused with 50 mL of PBS (1×). Brains were dissected aseptically, weighed, photographed and placed in 1 mL N, N-dimethylformamide for 48 hours at room temperature to extract dye from tissue. Absorbance was measured at 620 nm. The concentration was calculated using a standard curve of EB dye and expressed as ng dye per gram of brain tissue.

Detection of Cytokine Markers of Endothelial Activation

Peripheral whole blood was collected by saphenous venipuncture on day 0 (d 0; prior to PbA infection) and d 6 p.i. into heparinized tubes (Starstedt). Plasma was isolated from whole blood samples by centrifugation at 1000×g for 15 min. Plasma samples were aliquoted and stored at −80° C. until analyzed. Levels of mouse intercellular adhesion molecule-1 (sICAM-1/CD54), E-Selectin (sE-Sel/CD62E) and Vascular Cell Adhesion Molecule-1 (sVCAM-1/CD106) in their soluble forms were determined in plasma using commercially available murine ELISA kits (R&D Systems, Minneapolis, USA), according to the manufacturers protocol. Levels of von Willebrand Factor antigen (vWF:Ag) was measured in serum by ELISA as follows: 96-well MaxiSorp plates (Nunc) were coated overnight at 4° C. with a polyclonal antibody anti-human vWF (1:600, Dako, Glostrup, Denmark) in 0.01M PBS. Mouse serum was plated in 1% BSA-PBS and bound vWF:Ag was detected with horseradish peroxidase (HRP)-conjugated polyclonal antibody anti-human vWF (1:8000, Dako). Plates were developed with a 3,3′,5,5′-tetramethylbenzidine (TMB) substrate solution and the absorbance was read at 450 nm, after the colorimetric reaction was stopped with H₂SO₄. vWF:Ag concentration was interpolated from a standard curve created with human vWF of a known concentration from fresh frozen plasma (1:500, American Diagnostica, Stamford, Conn.) that was included on each plate. IFN-gamma and TNF-alpha were determined in plasma using commercially available murine ELISA kits (eBioscience), according to the manufacturer's protocol.

Statistical Analysis

Statistical analysis was performed using GraphPad Prism version 4.00 (San Diego, Calif.). Post-infection survival of mice was plotted as Kaplan Meier curves and assessed using log-rank test. Survival studies were conducted in triplicate and data pooled unless otherwise specified. Shapiro-Wilk test was used to determine normally distributed data and comparisons between groups were assessed using the non-parametric Mann-Whitney test or Kruskal-Wallis test followed by Dunn's post-hoc. Two-way ANOVA was used to compare between groups over multiple time-points. For plasma biomarker testing, the Friedman test with Dunn's multiple comparison was used to compare levels between samples collected from patients at different time points (e.g., admission and convalescence). All data are presented as median and IQR (non-parametric), unless otherwise stated. Normally distributed data is presented as mean and SEM. A p<0.05 was considered statistically significant. Data from multiple experiments were normalized to the geometric mean of the infected but untreated group of each experiment for comparisons.

Results

As shown in FIG. 1, the resistant BALB/c mice (also referred to as “ECM-R”) showed significantly prolonged survival (p=0.0007, log rank test) following infection with PbA as compared to the susceptible C57Bl/6 mice (also referred to as “ECM-S”). The resistant BALB/c mice showed 100% survival for 7 days post infection with survival dropping to more than 10% by Day 10 and up to Day 14 (when the mice were sacrificed). In contrast, the susceptible C57Bl/6 mice showed only about 50% survival as early as Day 6 with 0% by Day 8 post infection.

The ECM-S mice showed neurological impairment as evidenced by scores less than 35% around Day 6 as compared to the resistant ECM-R mice which showed an absence of neurological impairment (FIG. 2). Evans Blue (EB) extravasation was used to assess vascular permeability and blood-brain-barrier dysfunction. Following perfusion to remove circulating dye, extravasated EB level in brain parenchyma of PbA-infected ECM-S mice was 2-fold higher than level in ECM-R mice with comparable parasite burdens [mean (SD) EB dye/g tissue: 10.7 (7.9) for ECM-R mice vs. 22.9 (7.2) for ECM-S mice; p=0.005], consistent with increased vascular leakage and loss of blood-brain-barrier integrity (FIG. 3). This was independent of observed parasitemia as evidenced by a greater parasite burden in the resistant mice as compared to the susceptible mice (FIG. 4).

The ECM-R mice differed from the ECM-S mice in the levels of angiogenic factors Ang1, Ang2 and vWF upon PbA infection. Longitudinal evaluation over the course of infection showed that Ang1 levels decreased with time (p<0.0001, 2-way ANOVA; FIG. 5). The kinetics of Ang1 decline following infection was significantly different in ECM-R vs. ECM-S mice (p=0.02, 2-way ANOVA). During the acute phase of disease, ECM-R mice maintained significantly higher Ang1 levels as compared to ECM-S mice (p<0.001). For both strains, the loss of circulating Ang1 was associated with the onset of neurological impairment and ECM as determined by a significant decline in the RMCBS. Ang1 serum levels (ng/ml) correlated significantly with RMCBS (%) scores (p<0.05; FIG. 6a ) and with time to death (hours) (p<0.0001; FIG. 6b ). Overall, when assessed on day 6 post-infection, mice with lowest levels of circulating Ang1 were significantly more likely to proceed to a fatal outcome, supporting the hypothesis that Ang1 may be a critical determinant of survival.

The ECM-R mice showed significantly lower Ang2 and vWF levels (FIGS. 7-9).

Example 2: Blocking Ang2 does not Confer Improved Protection Against the Development of Experimental CM

In this Example, the effect of Ang2 blockade on PbA-induced ECM in a mouse model was assessed. Twenty C57Bl/6 mice were infected by Plasmodium berghei ANKA (PbA) via an intraperitoneal injection of 1×10⁶ freshly-isolated parasitized erythrocytes (PE) obtained from donor passage mice on Day 0. The infected mice were treated with 15 mg/kg of an anti-Ang2 antibody, H1H685, as described in US Patent Application Publication No. US20110027286, on Days −1, 1, 4, and 7 post-infection via subcutaneous injection. The mice were monitored for survival, neurological impairment, parasite burden and plasma protein levels, as described in detail in Example 1.

FIG. 10 shows a Kaplan Meier curve plotting the survival of mice infected with PbA and treated with anti-Ang2 antibody (referred to as “mAb ‘B’” in FIG. 10), or an isotype control (mAb ‘A’) or saline. Blocking Ang2 with the anti-Ang2 antibody did not lead to increased survival of infected mice as compared to the isotype control. Treatment with anti-Ang2 antibody also did not prevent neurological impairment in the infected mice (FIG. 11), though there was no significant difference in the parasite burden between infected mice treated with anti-Ang2 antibody, the isotype control or saline (FIG. 12). The plasma protein levels of vWF, ICAM, VCAM and E-selectin did not differ significantly in the mice treated with the anti-Ang2 antibody, or isotype control (FIG. 13).

Example 3: Therapeutic Administration of Ang1 Significantly Improves Survival of Mice Infected with PbA

In this Example, the effect of Ang1 administration on PbA-induced ECM in a mouse model was studied. Eighty C57Bl/6 mice were infected by Plasmodium berghei ANKA (PbA) via an intraperitoneal injection of 1×10⁶ freshly-isolated parasitized erythrocytes (PE) obtained from donor passage mice on Day 0. The infected mice were divided into four groups and were treated with either 15 mg/kg of an anti-Ang2 antibody (see Example 2), a “comparator” dual blocking antibody of Ang1/Ang2 or an isotype control, or with 25 mg/kg of AngF1-Fc-F1 (SEQ ID NO: 2) via subcutaneous injection on Day 4 and Day 6 post infection. The “comparator” dual Ang1/Ang2 blocking antibody was the peptibody 2×Con4C (AMG386) as set forth in U.S. Pat. No. 7,205,275 (Amgen). The mice were monitored for survival, neurological impairment, parasite burden, and plasma protein levels, as described in detail in Example 1.

As shown in FIG. 14, therapeutic administration of AngF1-Fc-F1 to mice infected with PbA significantly improved survival (p<0.05, log rank test) compared to mice treated with the isotype control, anti-Ang2 antibody or the dual blocking antibody. The mice treated with AngF1-Fc-F1 showed more than 35% survival up to at least Day 15 p.i. as compared to the mice treated with the other three treatments which showed 0% survival by Day 8 post infection, though the percent parasitemia across all treatments was similar (FIG. 15). The treatment with AngF1-Fc-F1 also protected blood brain barrier integrity as shown by Evans Blue dye uptake (FIG. 16). The mice treated with AngF1-Fc-F1 showed significantly low amount of dye uptake (panel C of FIG. 16a ), consistent with maintenance of an intact blood brain barrier and reduced vascular permeability (p<0.05, Kruskal-Wallis), even though the percent parasitemia was similar (FIG. 16b ). This confirmed that exogenous Ang1 is sufficient to maintain blood-brain-barrier integrity following a lethal malaria challenge.

The therapeutic administration of AngF1-Fc-F1 also prevented ECM-associated morbidity and neurological impairment (FIG. 17), independent of changes to peripheral parasitemia (FIG. 18). By day 6 post-infection, the majority of control mice had progressed to ECM, whereas disease progression was mitigated in treated mice. Infected AngF1-Fc-F1-treated mice displayed similar weight loss to control-treated mice.

To determine whether vascular protection with AngF1-Fc-F1 occurred secondary to a reduction in inflammatory cytokines or whether protection was due to a direct enhancement of vascular stability in the face of a systemic inflammatory response, plasma samples from treated and untreated PbA-infected mice were assayed for key pro-inflammatory cytokines. PbA-infected mice showed a significant increase in TNF and IFNγ on day 6 post-infection (3-fold increase in TNF and a 60-fold increase in IFNγ compared to baseline, p<0.01 for both, one-way ANOVA) despite treatment. Treatment with AngF1-Fc-F1 did not affect levels of TNF or IFNγ, with both control and treated mice showing a similar up-regulation in response to infection (FIG. 19a ).

Pro-inflammatory cytokine stimulation and/or direct endothelial interactions with parasitized erythrocytes may contribute to a number of pathological events implicated in CM, including up-regulation of endothelial cell receptors that mediate parasite cytoadhesion. Disruption of parasite sequestration to host receptors via down-regulation of cell adhesion molecules (CAMs), such as ICAM-1 and/or vascular cellular adhesion molecule-1 (VCAM-1), may lessen microvascular obstruction and endothelial dysfunction. Therefore, the effect of Ang1 treatment on reduction of circulating levels of soluble forms of CAMS, considered as an indicator of endothelial activation and a pro-adhesive vascular phenotype, was investigated. Analysis of plasma samples collected on day 6 post-infection showed a 4-fold increase in circulating levels of sICAM-1 with PbA infection, compared to baseline (p<0.001, One-way ANOVA with Bonferroni test for multiple comparisons; FIG. 19c ). These levels were significantly reduced with Ang1 treatment compared to PbA-infected controls (p<0.05; FIG. 19c ). Similarly, sVCAM-1 levels significantly increased at day 6 post-infection with PbA (5-fold increase, p<0.001; FIGS. 19c ) and Ang1 treatment significantly reduced circulating levels of sVCAM-1 compared to PbA-infected controls (p<0.05, FIG. 19c ). These data indicate that Ang-1-Tie-2 interactions help to maintain vascular quiescence in the face of systemic inflammatory response, in part through preservation of an anti-adhesive vascular phenotype via down regulation of adhesion molecules.

This study showed that therapeutic administration of Ang1 (AngF1-Fc-F1), but not inhibition of Ang2 improved blood brain barrier integrity and survival. It supported investigation of pro-Ang1, but not inhibition of Ang2 as adjunctive therapy for cerebral malaria. Further, it is of interest that Ang1-based treatment was efficacious and preserved blood brain barrier integrity, despite a robust systemic pro-inflammatory response to infection. The data suggest that anti-inflammatory strategies may not be required to preserve vascular integrity and improve outcome in life-threatening infections associated with systemic inflammation.

In one further experiment, AngF1-Fc-F1 will be administered in combination with an anti-Tie2 antibody (as set forth in US20130209492) to infected susceptible C57Bl/6 mice to study the involvement of Tie2 in blocking the protective effect of AngF1-Fc-F1. The anti-Tie2 antibody may an activating (or agonist) antibody, e.g., it increases the binding of an angiopoietin and/or increases the activity of Tie2. It is expected that AngF1-Fc-F1 administered in combination with anti-Tie2 antibody will lead to lower survival of infected mice as compared to AngF1-Fc-F1 alone.

In another further experiment, AngF1-Fc-F1 will be used to treat resistant BALB/c mice infected with PbA to study the effect on survival, blood brain barrier integrity, neurological impairment, and plasma protein markers. It is expected that administration of AngF1-Fc-F1 will lead to improved protection of blood brain barrier integrity and survival of infected BALB/c mice.

In a third experiment, AngF1-Fc-F1 will be administered in combination with an anti-Tie2 antibody to infected resistant BALB/c mice to study if the resistant mice are rendered susceptible to ECM. It is expected that AngF1-Fc-F1 administered in combination with anti-Tie2 antibody will lead to lower survival of infected BALB/c mice as compared to AngF1-Fc-F1 alone.

Example 4: Therapeutic Administration of AngF1-Fc-F1 as Adjunctive Therapy in Combination with Artesunate

In this Example, the effect of administration of Ang-F1-Fc-F1 in combination with artesunate on PbA-induced ECM in a mouse model was studied. Twenty C57Bl/6 mice were infected by Plasmodium berghei ANKA (PbA) via an intraperitoneal injection of 1×10⁶ freshly-isolated parasitized erythrocytes (PE) obtained from donor passage mice on Day 0. The infected mice were treated with 15 mg/kg of AngF1-Fc-F1 (SEQ ID NO: 2) on Days 4 and 6 post infection and with 10 mg/kg of artesunate on Day 5 post-infection via subcutaneous injection. The mice were monitored for survival, neurological impairment, parasite burden, and plasma protein levels, as described in detail in Example 1.

Adjunctive AngF1-Fc-F1 treatment significantly improved survival of infected mice as compared to artesunate alone (FIG. 20). Infected mice treated with AngF1-Fc-F1 in combination with artesunate showed 100% survival at least up to Day 15 post infection. In contrast, infected mice treated with artesunate alone showed less than 60% survival by Day 8 post infection. Despite significantly diminished parasite burden to pre-ECM levels (i.e., <2% parasitemia), 41.7% of artesunate treated mice died of ECM. This effect was independent of percent parasitemia (FIG. 21).

In a further experiment, the effect of adjunctive AngF1-Fc-F1 in combination with artesunate will be studied on neurological impairment in infected mice. It is expected that administration of AngF1-Fc-F1 in combination with artesunate will prevent neurological impairment in infected mice as compared to artesunate alone.

In another further experiment, AngF1-Fc-F1 will be administered in combination with an anti-Ang2 antibody (as described in Example 2) to study survival of infected mice. It is expected that AngF1-Fc-F1 administered in combination with anti-Ang2 antibody will lead to improved survival of infected mice as compared to AngF1-Fc-F1 alone.

Example 5: Protection from Malaria-Associated Acute Lung Injury

In this Example, the effect of AngF1-Fc-F1 administration on vascular permeability in lung and malaria-associated acute lung injury in infected mice will be studied. Twenty C57Bl/6 mice will be infected with Plasmodium berghei ANKA (PbA) via an intraperitoneal injection of 1×10⁶ freshly-isolated parasitized erythrocytes (PE) obtained from donor passage mice on Day 0. The infected mice will be treated with 15 mg/kg of AngF1-Fc-F1 (SEQ ID NO: 2) on Days 4, and 6 post-infection via subcutaneous injection. The mice will be monitored for survival and vascular permeability in lung by Evans Blue staining.

It is expected that mice treated with AngF1-Fc-F1 will show absence of Evans Blue dye uptake in lungs pointing to absence of vascular permeability and protection from malaria-associated acute lung injury.

The present invention is not to be limited in scope by the specific embodiments described herein. Indeed, various modifications of the invention in addition to those described herein will become apparent to those skilled in the art from the foregoing description and the accompanying figures. Such modifications are intended to fall within the scope of the appended claims. 

What is claimed is:
 1. A method of increasing survival of a subject afflicted with a disease or disorder selected from the group consisting of severe cerebral malaria, experimental cerebral malaria, sepsis, dengue, hemorrhagic fever, toxic shock syndrome, hemorrhagic shock, hemolytic uremic syndrome, myocardial infarction and stroke, the method comprising administering a pharmaceutical composition comprising a therapeutically effective amount of a fusion protein comprising at least one fibrinogen-like domain of angiopoietin-1 fused to an immunoglobulin Fc fragment to the subject in need thereof.
 2. The method of claim 1, wherein the subject is infected with Plasmodium spp.
 3. The method of claim 1, wherein the administration of the fusion protein results in protection of the blood barrier integrity in the subject.
 4. The method of claim 1, wherein the administration of the fusion protein results in preventing at least one indication of neurological impairment in the subject.
 5. The method of claim 4, wherein the at least one indication of neurological impairment is selected from the group consisting of impaired balance or coordination, motor impairment, loss of reflexes and self-preservation, long term neurocognitive injury and impairment, memory deficits, affective disorders, lack of hygiene-related behavior, convulsion, and fitting.
 6. The method of claim 1, wherein the fusion protein is administered at a dose of 15 mg/kg of the subject's body weight.
 7. The method of claim 1, wherein the fusion protein is administered subcutaneously.
 8. The method of claim 1, wherein the fusion protein is administered in combination with a second therapeutic agent.
 9. The method of claim 8, wherein the second therapeutic agent is artesunate.
 10. The method of claim 1, wherein the fusion protein comprises a first fibrinogen-like domain of angiopoietin-1 fused at its C-terminal end to the N-terminal end of an Fc fragment and the Fc fragment fused at its C-terminal end to the N-terminal end of a second fibrinogen-like domain of angiopoietin-1.
 11. The method of claim 1, wherein the fusion protein is AngF1-Fc-F1.
 12. The method of claim 1, wherein the fusion protein comprises the amino acid sequence of SEQ ID NO:
 2. 13. The method of claim 1, wherein the fusion protein specifically binds a Tie1 receptor or a Tie2 receptor. 